Li metal batteries have been considered a promising alternative to Li-ion batteries because of the high theoretical capacity of the Li metal. There have been remarkable improvements in the electrochemical performance of Li metal electrodes, although the current Li metal technology is not sufficiently practical in terms of cycle performance, safety, and volume change during cycling. Herein, the role of pore size distribution in the Li metal plating behavior of porous frameworks is clarified to attain the ideal pore structure of the framework as a Li metal host. The monodisperse pore framework shows the conformal electrodeposition of the Li metal, whereas the pore size gradient framework exhibits the superconformal plating of the Li metal. The conformal and superconformal electrodepositions of the Li metal are elucidated in terms of variations along the pore depth direction in the charge-transfer resistance on the pore walls and the ionic resistance of electrolytes confined in pores. The pore size gradient framework also shows excellent electrochemical performance, such as stable capacity retention over 760 cycles with 0.5 mAh cm-2 at 2 mA cm-2. These findings provide fundamental insights into strategies to improve the electrochemical performance of porous frameworks for Li metal batteries.
Keywords: lithium dendrite; lithium metal; pore structure; superconformal electrodeposition; three-dimensional porous framework.